Quick answers
- What is Pyridoxine Hci?
- Pyridoxine Hci is a brand name of Pyridoxine hci, a prescription medicine. The FDA NDC Directory lists 1 Pyridoxine Hci product in 1 strength and form.
- Who makes Pyridoxine Hci?
- Fresenius Kabi USA holds the FDA application for Pyridoxine Hci (ANDA080618, approved August 14, 1972).
- Is there a generic or store brand of Pyridoxine Hci?
- Yes. The FDA NDC Directory lists 1 other product with the same active ingredients, strength and form as a Pyridoxine Hci product, 1 of them generic. Ask your pharmacist whether one is right for you.
- Has Pyridoxine Hci been recalled?
- No recall linked to Pyridoxine Hci products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Pyridoxine Hci is
Each Pyridoxine Hci product as listed in the FDA NDC Directory, by active ingredient, strength and form, with its official label. “Same medicine, other names” counts the other products with exactly the same active ingredients, strength and form (generic versions, store brands and other brands); inactive ingredients can differ.
Pyridoxine hci · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| pyridoxine hydrochloride 100 mg/mL injection, solution (intramuscular, intravenous) | Pyridoxine Hci | 1 product, 1 company | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Pyridoxine hci →
FDA approval
- ANDA: Abbreviated New Drug Application: how a generic version is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| ANDA080618 | Fresenius Kabi USA | August 14, 1972 | 1 |
Companies that list Pyridoxine Hci
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Pyridoxine Hci products.
Recalls
No recall linked to Pyridoxine Hci products (by their NDC code or label) appears in the FDA enforcement reports.
Sources
- NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
- NADAC (National Average Drug Acquisition Cost) 2026 — Centers for Medicare & Medicaid Services (CMS), data.medicaid.gov, list of November 4, 2026, retrieved November 7, 2026
Which names get a brand page: a name the NDC Directory lists for a medicine, held by one company (the FDA application holder, or the company named on most of its products), that is not just a description, and that is not the only product of its medicine.